International Journal of Medical and Pharmaceutical Research
2024, Volume-5, Issue-1 doi: 10.5281/zenodo.10608689
Original Article
Detection of ermB Mediating Erythromycin Resistance in Clinical Isolates of Enterococci
 ,
 ,
 ,
 ,
Published
Jan. 31, 2024
Abstract

Background: Enterococci are nosocomial pathogen. Their pathogenic potential has been attributed to their ability to resist antimicrobial drugs intrinsically, acquire and distribute antibiotic resistance determinants and adapt to changing environments. Linezolid resistance occurs by the mutations in the domain V of 23S rRNA, the presence of the cfr gene or mutations in the L3 and L4 ribosomal proteins. Erythromycin resistance is mainly due to target-site modification by the rRNAmethylating enzyme encoded by the erm gene or mediated by efflux pump mechanisms. This study aimed to detect and characterize the antimicrobial resistance mechanism to oxazolidinone (linezolid) and macrolide (erythromycin) among clinical isolates of Enterococci. Studies describing theresistance to erythromycin and linezolid are limited.

Objective: This study aimed to detect and characterize the antimicrobial resistance mechanismto oxazolidinone (linezolid) and macrolide (erythromycin) among clinical isolates of Enterococci.

Materials and Methods: A total number of 150 clinical isolates were included in this study. Susceptibility to various antibiotics was determined by disc diffusion. Minimum Inhibitory Concentration (MIC) was ascertained by agar dilution method for linezolid and erythromycin. Polymerase chain reaction was done to detect the genes, ermB and cfr that encode for erythromycin and linezolid respectively.

Results: Among 150 isolates, predominant were Enterococcus faecalis 116 (77%)  followed by  Enterococcus faecium 34 (23%). Of the 150 study isolates, the susceptibility to ampicillin was 64.6% (97/150), high level gentamicin 47% (70/150), linezolid (100%) and vancomycin (100%). Of the 90 exudative enterococcal isolates, only 13 were susceptible to erythromycin. Of the 77 erythromycin resistant isolates, ermB gene was detected in 42 and exhibited a high levelresistance with >32 mg/ml. The gene encoding for linezolid resistance, cfr was not detected in any of the study isolates.

Conclusion: High level resistance to erythromycin is mediated by ermB. Vancomycin and linezolid resistance were not encountered in the study. However, continuous monitoring of antimicrobial resistance of Enterococcus species is necessary to provide a guide for the appropriate selection of antibiotics for treatment and to implement preventive measures. 

Recommended Articles
Loading Image...
Volume-5, Issue-1
Citations
1299 Views
255 Downloads
Share this article
License
Copyright (c) International Journal of Medical and Pharmaceutical Research
pdf Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.
All papers should be submitted electronically. All submitted manuscripts must be original work that is not under submission at another journal or under consideration for publication in another form, such as a monograph or chapter of a book. Authors of submitted papers are obligated not to submit their paper for publication elsewhere until an editorial decision is rendered on their submission. Further, authors of accepted papers are prohibited from publishing the results in other publications that appear before the paper is published in the Journal unless they receive approval for doing so from the Editor-In-Chief.
IJMPR open access articles are licensed under a Creative Commons Attribution-ShareAlike 4.0 International License. This license lets the audience to give appropriate credit, provide a link to the license, and indicate if changes were made and if they remix, transform, or build upon the material, they must distribute contributions under the same license as the original.
Logo
International Journal of Medical and Pharmaceutical Research
About Us
The International Journal of Medical and Pharmaceutical Research (IJMPR) is an EMBASE (Elsevier)–indexed, open-access journal for high-quality medical, pharmaceutical, and clinical research.
Follow Us
© Copyright IJMPR | All Rights Reserved